GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11895 in Dinoroseobacter shibae DFL-12

Align Inositol transport system permease protein (characterized)
to candidate 3607106 Dshi_0528 Monosaccharide-transporting ATPase (RefSeq)

Query= reanno::WCS417:GFF2333
         (340 letters)



>FitnessBrowser__Dino:3607106
          Length = 334

 Score =  172 bits (437), Expect = 8e-48
 Identities = 107/313 (34%), Positives = 175/313 (55%), Gaps = 12/313 (3%)

Query: 27  FLVLIGIGLVFELFGWIVRDQSFLMNSQRLVLMILQVSIIGLLAIGVTQVIITTGIDLSS 86
           F +LI +  VF L   +  D+   ++SQ L  M  Q     +LA+ +T  ++T GIDLS 
Sbjct: 14  FRLLIIMVFVFGLMSVLSPDR--FLSSQNLTSMAFQFPEFAILALAMTIAMMTGGIDLSV 71

Query: 87  GSVLALSAMIAASLAQTSDFSRAVFPSLTDLPVWIPVAM--GLGVGLLAGAINGSIIAVT 144
             +  LSA++AA +   + FS A  P+     +W+ +A+   L +G +AG INGS++A  
Sbjct: 72  VGIANLSAVVAALIL--THFSNAEMPAAQSA-IWLAIAITAALCIGAIAGLINGSLVAFF 128

Query: 145 GIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIGHGAM-----PVIIFLVVAVIF 199
           G+PP +ATLG  +   G A   T G  V    D+   IG+  +     P+I+F V+A + 
Sbjct: 129 GLPPILATLGSGLVFTGFAIAMTGGSAVMGFPDTVALIGNATLAGVPVPLILFAVLAFLL 188

Query: 200 HIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLIIVYSIAGLLAGLAGVVASARAATGQ 259
           H+ L  T +G      G N  AA  + I++ R L+ VY IAG+ A +AG++  +RA + +
Sbjct: 189 HLVLTRTAFGLRVTMYGANPLAALYAAIDINRMLLKVYVIAGMFASVAGLIIMSRANSAK 248

Query: 260 AGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVMASGFTFVGVDAYIQDIIK 319
           A  G SY L A+  AV+GG +  GG GR+ G V+  L +  ++SG   +GV  + +++I 
Sbjct: 249 ADYGSSYLLLAVLIAVLGGVNPYGGYGRVIGVVLAVLSMQFLSSGLNMLGVSNFARELIW 308

Query: 320 GLIIVVAVVIDQY 332
           G ++++ +VI+ +
Sbjct: 309 GALLILVMVINTH 321


Lambda     K      H
   0.325    0.140    0.394 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 230
Number of extensions: 12
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 340
Length of database: 334
Length adjustment: 28
Effective length of query: 312
Effective length of database: 306
Effective search space:    95472
Effective search space used:    95472
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory